Evaluating RANKL and OPG levels in patients with Duchenne muscular dystrophy

被引:8
作者
Ali, S. Akhtar [1 ]
Kang, H. [2 ]
Olney, R. [3 ]
Ramos-Platt, L. [4 ]
Ryabets-Lienhard, A. [1 ]
Cheung, C. [1 ]
Georgia, S. [5 ,6 ,7 ]
Pitukcheewanont, P. [1 ]
机构
[1] CHLA, Ctr Endocrinol Diabet & Metab, 4650 Sunset Blvd 61, Los Angeles, CA 90027 USA
[2] Univ Southern Calif, Los Angeles, CA USA
[3] Nemour Childrens Hosp, Div Endocrinol, Jacksonville, FL USA
[4] CHLA, Ctr Neurol, Los Angeles, CA USA
[5] CHLA, Saban Res Inst, Los Angeles, CA USA
[6] CHLA, Ctr Endocrinol Diabet & Metab, Diabet & Obes Program, Los Angeles, CA USA
[7] USC, Keck Sch Med, Los Angeles, CA USA
关键词
Muscular dystrophy; OPG; Osteoporosis; RANKL; X-RAY ABSORPTIOMETRY; CHILDREN; OSTEOPROTEGERIN; ADOLESCENTS; DENSITY;
D O I
10.1007/s00198-019-05077-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A Summary RANKL-OPG should be explored in DMD patients to potentially provide targeted therapy. We quantified RANKL and OPG levels in DMD patients compared with controls. RANKL, OPG, and RANKL:OPG significantly declined with age in DMD patients suggesting some bone turnover markers are difficult to assess or use as therapeutic indicators. Introduction Osteoporosis in Duchenne muscular dystrophy (DMD) is multi-factorial in nature with high prevalence of fractures. RANKL-OPG should be explored to potentially provide targeted therapy for these patients. We quantified RANKL, OPG, and RANKL:OPG levels in DMD patients compared with controls and analyzed the influence of age, glucocorticoid use, ambulatory status, bone density, and fracture history. Methods DMD patients were enrolled at CHLA. Controls were recruited from general pediatric clinic and in collaboration with samples from a previously completed study. Free soluble RANKL and OPG levels were quantified using a sandwich ELISA. Results Fifty DMD patients and 50 controls were enrolled. DMD patients had a significant decline in RANKL, OPG, and RANKL:OPG with age (p = < 0.0001, p = 0.026, and p = 0.002, respectively) while healthy controls showed no significant change. RANKL trended lower in patients on glucocorticoids (p = 0.05), attributed to the significantly older age in the treatment group. RANKL and RANKL:OPG levels were significantly lower in the non-ambulatory group compared with the ambulatory group (p = 0.010 and 0.036 respectively), again likely due to their older age. There was no correlation of RANKL, OPG, or RANKL:OPG with DXA Z-score or presence of vertebral fractures. Conclusion There was significant decline in RANKL, OPG, and RANKL:OPG with age in DMD patients compared with controls, potentially due to disease severity or worsening osteoblastic function. This suggests some bone turnover markers may be difficult to assess or use as therapeutic indicators in DMD patients. Larger studies are needed to evaluate the role of RANKL-OPG in DMD patients to provide better targeted therapy.
引用
收藏
页码:2283 / 2288
页数:6
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